College of Pharmacy, Sookmyung Women's University, Seoul, Korea.
College of Natural Sciences, Kyungpook National University, Daegu, Korea.
FEBS Lett. 2021 Jan;595(1):58-67. doi: 10.1002/1873-3468.13963. Epub 2020 Nov 10.
Dynamin-related protein 1 (DRP1) is a mitochondrial membrane GTPase and regulates mitochondrial fission. In this study, we found that the cytokine RANKL increased the expression of DRP1 and its receptor proteins, Fis1, Mid49, and Mid 51, during osteoclast formation in mouse bone marrow-derived macrophages. Inactivation of the kinase GSK3β appeared to induce DRP1 expression. DRP1 knockdown or the DRP1 inhibitor Mdivi1 suppressed osteoclast differentiation via downregulation of c-Fos and NFATc1, the key transcription factor for osteoclast formation. Finally, the DRP1 inhibitor suppressed lipopolysaccharide-induced osteoclast formation in a calvarial model and ovariectomy-induced bone loss in vivo. Taken together, our data demonstrate that DRP1 positively contributes to RANKL-induced osteoclast differentiation by regulating the c-Fos-NFATc1 axis, suggesting the importance of mitochondrial DRP1 in osteoclastogenesis.
动力相关蛋白 1(DRP1)是一种线粒体膜 GTP 酶,调节线粒体裂变。在这项研究中,我们发现细胞因子 RANKL 在小鼠骨髓来源巨噬细胞的破骨细胞形成过程中增加了 DRP1 及其受体蛋白 Fis1、Mid49 和 Mid51 的表达。激酶 GSK3β 的失活似乎会诱导 DRP1 的表达。DRP1 敲低或 DRP1 抑制剂 Mdivi1 通过下调破骨细胞形成的关键转录因子 c-Fos 和 NFATc1 来抑制破骨细胞分化。最后,DRP1 抑制剂抑制脂多糖诱导的颅骨模型中的破骨细胞形成和体内去卵巢诱导的骨丢失。总之,我们的数据表明,DRP1 通过调节 c-Fos-NFATc1 轴正向促进 RANKL 诱导的破骨细胞分化,提示线粒体 DRP1 在破骨细胞生成中的重要性。